Drug Development Meetings
Join FDAnews Thursday, May 19, for a 90-minute audioconference on "Preparing Successful eCTDs: Compliant Submissions the First Time, Every Time." Learn how to correctly prepare your electronic common technical documents to the FDA's expectations. On May 20, join FDAnews for "Voluntary No More -- California's New Mandatory Rules for Drug and Device Firms: Compliance and Marketing Strategies to Meet Your July 1 Deadline." Learn about the landmark legislation that is changing the rules for drugmakers and devicemakers in California, the key components for meeting the deadline, and how others are complying.
May 16-18: Clinical Data Management
Philadelphia, Pa.
(703) 276-0178
Peri
maria.simonetti@peri.org
www.peri.org
May 17-18: Improving Investigator and Site Management Using CTMS
Webcast
(609) 524-4100
ClinPhone
info@clinphone.com
www.clinphone.com
May 18-19: GLP Training
Philadelphia, Pa.
(443) 543-5530
SPI USA
seminars@usaspi.com
www.usaspi.com
May 18-19: Innovation Boot Camp
Newport Beach, Calif.
(714) 289-1233
Institute for Effective Innovation
info@innovationbootcamp.com
www.InnovationBootCamp.com
May 18-19: Parenteral Product Development
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation & Education
lcourville@cfpie.com
www.cfpie.com
May 18-20: Advanced Good Clinical Practices
Bethesda, Md.
(703) 276-0178
Peri
maria.simonetti@peri.org
www.peri.org
May 19: Preparing Successful eCTDs
Compliant Submissions the First Time, Every Time
Your Office
An audioconference
(703) 538-7600
FDAnews
www.fdanews.com/wbi/conferences/ectd.html (http://www.fdanews.com/wbi/conferences/ectd.html)
May 19-20: Risk-Based Approach to Computer Compliance Focusing on Clinical Trials
Phoenix, Ariz.
(919) 531-5369
SEC Associates and SAS
Dori.Pyles@SAS.com
http://support.sas.com/training/us/crs/bracc.html
May 20: Voluntary No More -- California's New Mandatory Rules for Drug and Device Firms
Compliance and Marketing Strategies to Meet Your July 1 Deadline
An audioconference
Your Office
(703) 538-7600
FDAnews
www.fdanews.com/wbi/conferences/californialaw.html (http://www.fdanews.com/wbi/conferences/californialaw.html)
May 23-25: 15th International Contracting and Negotiating Clinical Trials
Philadelphia, Pa.
(212) 967-0095
Strategic Research Institute
sgrodsky@srinstitute.com
www.srinstitute.com/cs317
May 23-25: IIR's Optimizing Preclinical Outsourcing
Boston, Mass.
(212) 661-3500
Institute for International Research
slee@iirusa.com
www.iirusa.com/preclinicaloutsourcing
May 24: Reduce Supply Chain Risks
How the FDA Expects You to Manage Outsourced Suppliers
An FDAnews audioconference With Martin Browning
Your Office
(703) 538-7600
FDAnews
www.fdanews.com/wbi/conferences/supplychain.html (http://www.fdanews.com/wbi/conferences/supplychain.html)
May 24-25: CHI's Third Annual R&D Strategies: Managing Risk to Increase Productivity
Philadelphia, Pa.
(617) 630-1300
Cambridge Healthtech Institute
chi@healthtech.com
http://www.worldpharmacongress.com/
May 24-25: Monitoring of Clinical Trials
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation & Education
info@cfpie.com
www.cfpie.com
May 24-26: CHI's World Pharmaceutical Congress
Philadelphia, Pa.
(617) 630-1300
Cambridge Healthtech Institute
chi@healthtech.com
www.healthtech.com
May 25: Deviation Investigation Report Writing
Somerset, N.J.
(801) 685-7717 x306
McCulley/Cuppan
jgregg@mcculley-cuppan.com
www.mcculley-cuppan.com
May 25: FDA's New Risk Management Guidances
Roadmaps and RiskMAPs for Improving Drug Safety
An audioconference
Your Office
(703) 538-7600
FDAnews
www.fdanews.com/wbi/conferences/riskmaps.html (http://www.fdanews.com/wbi/conferences/riskmaps.html)